Disease #06757 (OZEMA5;OOMD (ocyte/zygote/embryo maturation arrest, type 5), OMIM:617996)
| Official abbreviation |
OZEMA5;OOMD |
| Name |
ocyte/zygote/embryo maturation arrest, type 5 |
| OMIM ID |
617996 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
WEE2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-12-10 23:20:41 +01:00 (CET) |
| Date last edited |
2024-11-08 11:48:51 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|